These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

123 related articles for article (PubMed ID: 17485165)

  • 1. Short half-lives of ataxia-associated aprataxin proteins in neuronal cells.
    Hirano M; Asai H; Kiriyama T; Furiya Y; Iwamoto T; Nishiwaki T; Yamamoto A; Mori T; Ueno S
    Neurosci Lett; 2007 May; 419(2):184-7. PubMed ID: 17485165
    [TBL] [Abstract][Full Text] [Related]  

  • 2. DNA single-strand break repair is impaired in aprataxin-related ataxia.
    Hirano M; Yamamoto A; Mori T; Lan L; Iwamoto TA; Aoki M; Shimada K; Furiya Y; Kariya S; Asai H; Yasui A; Nishiwaki T; Imoto K; Kobayashi N; Kiriyama T; Nagata T; Konishi N; Itoyama Y; Ueno S
    Ann Neurol; 2007 Feb; 61(2):162-74. PubMed ID: 17315206
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein.
    Sano Y; Date H; Igarashi S; Onodera O; Oyake M; Takahashi T; Hayashi S; Morimatsu M; Takahashi H; Makifuchi T; Fukuhara N; Tsuji S
    Ann Neurol; 2004 Feb; 55(2):241-9. PubMed ID: 14755728
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Early-onset ataxia with ocular motor apraxia and hypoalbuminemia/ataxia with oculomotor apraxia 1.
    Tada M; Yokoseki A; Sato T; Makifuchi T; Onodera O
    Adv Exp Med Biol; 2010; 685():21-33. PubMed ID: 20687492
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The FHA domain of aprataxin interacts with the C-terminal region of XRCC1.
    Date H; Igarashi S; Sano Y; Takahashi T; Takahashi T; Takano H; Tsuji S; Nishizawa M; Onodera O
    Biochem Biophys Res Commun; 2004 Dec; 325(4):1279-85. PubMed ID: 15555565
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Aprataxin (APTX) gene mutations resembling multiple system atrophy.
    Baba Y; Uitti RJ; Boylan KB; Uehara Y; Yamada T; Farrer MJ; Couchon E; Batish SD; Wszolek ZK
    Parkinsonism Relat Disord; 2007 Apr; 13(3):139-42. PubMed ID: 17049295
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia.
    Yokoseki A; Ishihara T; Koyama A; Shiga A; Yamada M; Suzuki C; Sekijima Y; Maruta K; Tsuchiya M; Date H; Sato T; Tada M; Ikeuchi T; Tsuji S; Nishizawa M; Onodera O
    Brain; 2011 May; 134(Pt 5):1387-99. PubMed ID: 21486904
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nucleolar localization of aprataxin is dependent on interaction with nucleolin and on active ribosomal DNA transcription.
    Becherel OJ; Gueven N; Birrell GW; Schreiber V; Suraweera A; Jakob B; Taucher-Scholz G; Lavin MF
    Hum Mol Genet; 2006 Jul; 15(14):2239-49. PubMed ID: 16777843
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Aprataxin mutations are a rare cause of early onset ataxia in Germany.
    Habeck M; Zühlke C; Bentele KH; Unkelbach S; Kress W; Bürk K; Schwinger E; Hellenbroich Y
    J Neurol; 2004 May; 251(5):591-4. PubMed ID: 15164193
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel splice variants increase molecular diversity of aprataxin, the gene responsible for early-onset ataxia with ocular motor apraxia and hypoalbuminemia.
    Hirano M; Nishiwaki T; Kariya S; Furiya Y; Kawahara M; Ueno S
    Neurosci Lett; 2004 Aug; 366(2):120-5. PubMed ID: 15276230
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel nonsense mutation in the APTX gene associated with delayed DNA single-strand break removal fails to enhance sensitivity to different genotoxic agents.
    Crimella C; Cantoni O; Guidarelli A; Vantaggiato C; Martinuzzi A; Fiorani M; Azzolini C; Orso G; Bresolin N; Bassi MT
    Hum Mutat; 2011 Apr; 32(4):E2118-33. PubMed ID: 21412945
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Purkinje cell loss in the cerebellar flocculus in patients with ataxia with ocular motor apraxia type 1/early-onset ataxia with ocular motor apraxia and hypoalbuminemia.
    Sugawara M; Wada C; Okawa S; Kobayashi M; Sageshima M; Imota T; Toyoshima I
    Eur Neurol; 2008; 59(1-2):18-23. PubMed ID: 17917453
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The gene mutated in ataxia-ocular apraxia 1 encodes the new HIT/Zn-finger protein aprataxin.
    Moreira MC; Barbot C; Tachi N; Kozuka N; Uchida E; Gibson T; Mendonça P; Costa M; Barros J; Yanagisawa T; Watanabe M; Ikeda Y; Aoki M; Nagata T; Coutinho P; Sequeiros J; Koenig M
    Nat Genet; 2001 Oct; 29(2):189-93. PubMed ID: 11586300
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cerebellar ataxia with oculomotor apraxia type 1: clinical and genetic studies.
    Le Ber I; Moreira MC; Rivaud-Péchoux S; Chamayou C; Ochsner F; Kuntzer T; Tardieu M; Saïd G; Habert MO; Demarquay G; Tannier C; Beis JM; Brice A; Koenig M; Dürr A
    Brain; 2003 Dec; 126(Pt 12):2761-72. PubMed ID: 14506070
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Aprataxin, a novel protein that protects against genotoxic stress.
    Gueven N; Becherel OJ; Kijas AW; Chen P; Howe O; Rudolph JH; Gatti R; Date H; Onodera O; Taucher-Scholz G; Lavin MF
    Hum Mol Genet; 2004 May; 13(10):1081-93. PubMed ID: 15044383
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations.
    Shimazaki H; Takiyama Y; Sakoe K; Ikeguchi K; Niijima K; Kaneko J; Namekawa M; Ogawa T; Date H; Tsuji S; Nakano I; Nishizawa M
    Neurology; 2002 Aug; 59(4):590-5. PubMed ID: 12196655
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Early-onset ataxia with oculomotor apraxia with a novel APTX mutation.
    Ito A; Yamagata T; Mori M; Momoi MY
    Pediatr Neurol; 2005 Jul; 33(1):53-6. PubMed ID: 15876520
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Loss of function mechanism in aprataxin-related early-onset ataxia.
    Hirano M; Furiya Y; Kariya S; Nishiwaki T; Ueno S
    Biochem Biophys Res Commun; 2004 Sep; 322(2):380-6. PubMed ID: 15325241
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ataxia with oculomotor apraxia type 1 (AOA1): clinical and neuropsychological features in 2 new patients and differential diagnosis.
    D'Arrigo S; Riva D; Bulgheroni S; Chiapparini L; Castellotti B; Gellera C; Pantaleoni C
    J Child Neurol; 2008 Aug; 23(8):895-900. PubMed ID: 18403580
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Short-patch single-strand break repair in ataxia oculomotor apraxia-1.
    Reynolds JJ; El-Khamisy SF; Caldecott KW
    Biochem Soc Trans; 2009 Jun; 37(Pt 3):577-81. PubMed ID: 19442253
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.